NDC 69349-104 Studio Blend Cover Foundation Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69349-104?
What are the uses for Studio Blend Cover Foundation Spf 15?
Which are Studio Blend Cover Foundation Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Studio Blend Cover Foundation Spf 15 Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- PEG/PPG-10/2 DIMETHICONE (UNII: 5GDV42659J)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".